Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western Pacific

We present the mixing ratio, δ<sup>13</sup>C and δD of atmospheric CH<sub>4</sub> using commercial aircraft in the upper troposphere (UT) over the Western Pacific for the period December 2005–September 2010. The obse...

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Main Authors: T. Umezawa, T. Machida, K. Ishijima, H. Matsueda, Y. Sawa, P. K. Patra, S. Aoki, T. Nakazawa
Format: Article
Language:English
Published: Copernicus Publications 2012-09-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/12/8095/2012/acp-12-8095-2012.pdf
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spelling doaj-844ead7ff8244b83a7761f62b32b05b12020-11-25T00:14:05ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242012-09-0112178095811310.5194/acp-12-8095-2012Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western PacificT. UmezawaT. MachidaK. IshijimaH. MatsuedaY. SawaP. K. PatraS. AokiT. NakazawaWe present the mixing ratio, δ<sup>13</sup>C and δD of atmospheric CH<sub>4</sub> using commercial aircraft in the upper troposphere (UT) over the Western Pacific for the period December 2005–September 2010. The observed results were compared with those obtained using commercial container ships in the lower troposphere (LT) over the same region. In the Northern Hemisphere (NH), the UT CH<sub>4</sub> mixing ratio shows high values in the boreal summer–autumn, when the LT CH<sub>4</sub> mixing ratio reaches a seasonal minimum. From tagged tracer experiments made using an atmospheric chemistry transport model, we found that such high CH<sub>4</sub> values are due to rapid transport of air masses influenced by CH<sub>4</sub> sources in South Asia and East Asia. The observed isotopic ratio data imply that these areas have CH<sub>4</sub> sources with relatively low δ<sup>13</sup>C and δD signatures such as biogenic sources. Latitudinal distributions of the annual average UT and LT CH<sub>4</sub> mixing ratio intersect each other in the tropics; the mixing ratio value is lower in the UT than in the LT in the NH and the situation is reversed in the Southern Hemisphere (SH), due mainly to the NH air intrusion into the SH through the UT. Such intersection of the latitudinal distributions is observable in δD but not in δ<sup>13</sup>C, implying an additional contribution from reaction of CH<sub>4</sub> with active chlorine in the marine boundary layer. δ<sup>13</sup>C and δD show low values in the NH and high values in the SH both in the UT and in the LT. We also observed an increase in the CH<sub>4</sub> mixing ratio and decreases in δ<sup>13</sup>C and δ<D during 2007–2008 in the UT and LT over the Western Pacific, possibly due to enhanced biogenic emissions in the tropics and NH.http://www.atmos-chem-phys.net/12/8095/2012/acp-12-8095-2012.pdf
collection DOAJ
language English
format Article
sources DOAJ
author T. Umezawa
T. Machida
K. Ishijima
H. Matsueda
Y. Sawa
P. K. Patra
S. Aoki
T. Nakazawa
spellingShingle T. Umezawa
T. Machida
K. Ishijima
H. Matsueda
Y. Sawa
P. K. Patra
S. Aoki
T. Nakazawa
Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western Pacific
Atmospheric Chemistry and Physics
author_facet T. Umezawa
T. Machida
K. Ishijima
H. Matsueda
Y. Sawa
P. K. Patra
S. Aoki
T. Nakazawa
author_sort T. Umezawa
title Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western Pacific
title_short Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western Pacific
title_full Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western Pacific
title_fullStr Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western Pacific
title_full_unstemmed Carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the Western Pacific
title_sort carbon and hydrogen isotopic ratios of atmospheric methane in the upper troposphere over the western pacific
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2012-09-01
description We present the mixing ratio, δ<sup>13</sup>C and δD of atmospheric CH<sub>4</sub> using commercial aircraft in the upper troposphere (UT) over the Western Pacific for the period December 2005–September 2010. The observed results were compared with those obtained using commercial container ships in the lower troposphere (LT) over the same region. In the Northern Hemisphere (NH), the UT CH<sub>4</sub> mixing ratio shows high values in the boreal summer–autumn, when the LT CH<sub>4</sub> mixing ratio reaches a seasonal minimum. From tagged tracer experiments made using an atmospheric chemistry transport model, we found that such high CH<sub>4</sub> values are due to rapid transport of air masses influenced by CH<sub>4</sub> sources in South Asia and East Asia. The observed isotopic ratio data imply that these areas have CH<sub>4</sub> sources with relatively low δ<sup>13</sup>C and δD signatures such as biogenic sources. Latitudinal distributions of the annual average UT and LT CH<sub>4</sub> mixing ratio intersect each other in the tropics; the mixing ratio value is lower in the UT than in the LT in the NH and the situation is reversed in the Southern Hemisphere (SH), due mainly to the NH air intrusion into the SH through the UT. Such intersection of the latitudinal distributions is observable in δD but not in δ<sup>13</sup>C, implying an additional contribution from reaction of CH<sub>4</sub> with active chlorine in the marine boundary layer. δ<sup>13</sup>C and δD show low values in the NH and high values in the SH both in the UT and in the LT. We also observed an increase in the CH<sub>4</sub> mixing ratio and decreases in δ<sup>13</sup>C and δ<D during 2007–2008 in the UT and LT over the Western Pacific, possibly due to enhanced biogenic emissions in the tropics and NH.
url http://www.atmos-chem-phys.net/12/8095/2012/acp-12-8095-2012.pdf
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